A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697131



Internal ID120797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89360639..89362747hg38UCSC Ensembl
chr14:89826983..89829091hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg382109
hg192109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144946
Supporting Variants
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697131
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002657


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